A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5722065



Internal ID9187999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88747268..88747531hg38UCSC Ensembl
chr8:89759497..89759760hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661524
Supporting Variants
SamplesHG01462
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5722065
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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